CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 15 enrolled
Drug / intervention
Microneedle patch +2 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02682056
NCT02682056N/ACompleted

Glucose Measurement Using Microneedle Patches

Emory University·interventional·Posted Feb 15, 2016·Updated Jan 3, 2020

In Brief

A clinical study evaluating Microneedle patch, Intravenous (IV) catheter, and 1 other intervention for Diabetes. Completed, enrolled 15 participants across 2 sites.

Detailed Summary

This study will compare three glucose measurement techniques among diabetic children and adolescents. The study seeks to determine if a microneedle patch (made from biocompatible polymers or metal), versus a lancet or intravenous catheter, would be a preferable option for monitoring glucose levels among the diabetic pediatric population.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDiabetes
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 15, 2016
Enrollment StartDec 21, 2017
Primary CompletionJan 29, 2018
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 10.4 years ago

Interventions

Microneedle patchdevice

The microneedle patch will collect interstitial fluid to be tested for glucose level. The microneedles are made from biocompatible polymers or metal. Participants will have fasting glucose levels measured four times, on an hourly basis, during the study visit.

Intravenous (IV) catheterdevice

The intravenous (IV) catheter will collect venous blood to be tested for glucose level. Participants will have fasting glucose levels measured four times, on an hourly basis, during the study visit.

Lancetdevice

The lancet will collect capillary blood to be tested for glucose level. Participants will have fasting glucose levels measured four times, on an hourly basis, during the study visit.